ORPHA:662255
Grisel syndrome
Synonyms: Atlantoaxial non-traumatic subluxation
- Type
- Clinical syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Childhood
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Grisel syndrome | Atlantoaxial non-traumatic subluxation |
| fr | Syndrome de grisel | Torticolis de Grisel · Torticolis naso-pharyngien · Torticolis nasopharyngien |
| de | Grisel-Syndrom | Atraumatische atlantoaxiale Subluxation |
| es | Síndrome de Grisel | Subluxación atlantoaxial no traumática |
| it | Sindrome di Grisel | Sublussazione atlanto-assiale non traumatica |
| nl | Syndroom van Grisel | Niet-traumatische subluxatie van atlanto-axiaal gewricht |
| pt | Síndrome Grisel | Subluxação atlantoaxial não-traumática |
| pl | Zespół Grisela | = en |
| cs | Griselův syndrom | = en |
| uk | Синдром Грізеля | Атлантоаксіальний нетравматичний підвивих |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M43.8 | NTBT | attributed | validated |
| ICD-11 | LB73.22 | NTBT | attributed | validated |
| MONDO | 0971080 | E | validated | |
| MONDO | 971080 | E | validated | |
| UMLS | C0263885 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:182231Rare rheumatologic disease
rare systemic and rheumatological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 173 cases | Worldwide | Case(s) | Validated | 33274097[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 33274097[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/662255
- This record as JSON: /data/d/662255.json